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Wei Gao
Wei Gao
University of South China
Cobalamin
Disease
Hereditary Diseases
Internal medicine
Urine organic acids
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Identification of MMACHC and PROKR2 mutations causing coexistent cobalamin C disease and Kallmann syndrome in a young woman.
2021
Metabolic Brain Disease
Haijun Yuan
Sipeng Deng
Wei Gao
Huaxin Li
Mei Yuan
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